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黄芪甲苷对 2 型糖尿病肾病大鼠内质网应激诱导的肾小管上皮细胞凋亡的保护作用。

Protective effects of Astragaloside IV on endoplasmic reticulum stress-induced renal tubular epithelial cells apoptosis in type 2 diabetic nephropathy rats.

机构信息

Key Laboratory of Anti-Inflammatory and Immunopharmacology, Ministry of Education, Department of Pharmacology, Anhui Medical University, Hefei 230032, Anhui, China.

Key Laboratory of Anti-Inflammatory and Immunopharmacology, Ministry of Education, Department of Pharmacology, Anhui Medical University, Hefei 230032, Anhui, China.

出版信息

Biomed Pharmacother. 2019 Jan;109:84-92. doi: 10.1016/j.biopha.2018.10.041. Epub 2018 Nov 2.

Abstract

Diabetic nephropathy (DN) has become the leading cause of end-stage renal disease (ESRD) worldwide. Renal tubular injury plays an important role in the development and progression of DN. And apoptosis of renal tubular epithelial cells (RTEC) contribute to the loss of renal function, increased levels of serum creatinine (SCr), blood urea nitrogen (BUN), urine total protein to urine creatinine and microalbuminuria and reduction of creatinine clear rate (CCr). Moreover, recent findings suggested that endoplasmic reticulum (ER) stress may lead to apoptosis of renal cells. Astragalosides IV (AS-IV) has a variety of pharmacological effects such as anti-apoptosis. Thus, in this study we investigated the effects and mechanisms of AS-IV on apoptosis of RTEC in high-fat diets (HFD) and low-dose streptozotocin (STZ)-induced type 2 DN rats. The results showed that AS-IV (40, 80 mg/kg) could alleviate RTEC apoptosis in DN rats. Furthermore, body weight, the majority of biochemical and renal function parameters and histopathological changes in the diabetic kidney were also improved by AS-IV. And AS-IV could reduce the expression of apoptosis-related proteins cleaved caspase-3, Bax/Bcl-2 ratio. ER stress-related proteins GRP78, p-PERK, ATF4 and CHOP were also inhibited by AS-IV in kidney of DN rats. Taken together, our study suggests that the protective effects of AS-IV may be related to inhibit ER stress-induced apoptosis through down-regulating the expression of p-PERK, ATF4 and CHOP. And our study provides a new theoretical basis for the clinical treatment of patients with kidney diseases.

摘要

糖尿病肾病(DN)已成为全球终末期肾病(ESRD)的主要原因。肾小管损伤在 DN 的发生和发展中起重要作用。肾小管上皮细胞(RTEC)的凋亡导致肾功能丧失、血清肌酐(SCr)、血尿素氮(BUN)、尿总蛋白与尿肌酐比值和微量白蛋白尿增加以及肌酐清除率(CCr)降低。此外,最近的研究结果表明,内质网(ER)应激可能导致肾细胞凋亡。黄芪甲苷 IV(AS-IV)具有多种药理作用,如抗凋亡。因此,在这项研究中,我们研究了 AS-IV 对高脂肪饮食(HFD)和低剂量链脲佐菌素(STZ)诱导的 2 型糖尿病肾病大鼠 RTEC 凋亡的影响及其机制。结果表明,AS-IV(40、80mg/kg)可减轻 DN 大鼠 RTEC 凋亡。此外,AS-IV 还改善了糖尿病肾脏中的体重、大多数生化和肾功能参数以及组织病理学变化。AS-IV 还可降低凋亡相关蛋白 cleaved caspase-3、Bax/Bcl-2 比值的表达。DN 大鼠肾脏中 ER 应激相关蛋白 GRP78、p-PERK、ATF4 和 CHOP 的表达也被 AS-IV 抑制。总之,我们的研究表明,AS-IV 的保护作用可能与通过下调 p-PERK、ATF4 和 CHOP 的表达抑制 ER 应激诱导的凋亡有关。我们的研究为肾脏疾病患者的临床治疗提供了新的理论依据。

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